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Neuropeptide

Bombesin

Bombesin is a 14-amino-acid peptide first isolated from amphibian skin that gave its name to a family of mammalian receptors. It is widely used as a research tool in appetite and receptor-biology studies.

By The Peptides Codex Editorial TeamIndividual review date not recorded

Page data last changed: . Registry refreshes and identity assessments are separate from scientific content review.

Reference backbone length
14 positions
Class
Neuropeptide
Function
Appetite and gastrin-release signaling (research)
Context
Neuroscience and receptor-imaging research

Amphibian peptide that defined the bombesin receptor family.

Part of the Neuropeptides & signaling cluster

Overview

Bombesin is a 14-amino-acid peptide first isolated from amphibian skin that gave its name to a family of mammalian receptors. It is widely used as a research tool in appetite and receptor-biology studies.

Source & context

Biological / chemical source: Originally isolated from frog (Bombina) skin

Primary research or clinical context: Neuroscience and receptor-imaging research

Receptor family it defined

Bombesin is the prototype for a receptor class whose mammalian members include the gastrin-releasing peptide receptor. Because these receptors are studied in tumor imaging, bombesin analogs appear frequently in radiopharmaceutical research literature.

Research-tool status

Bombesin is chiefly used as an experimental probe rather than a therapeutic. This page presents its receptor pharmacology for education and does not describe any human use.

Sequence of the selected reference form

Sequence backbone for the reference form: Bombina bombina bombesin(1-14), N-terminal L-pyroglutamate and C-terminal Met amide. Termini, stereochemistry and modifications are described below.

XQRLGNQWAVGHLM

XQRLGNQWAVGHLM

X positions L-pyroglutamate (5-oxoproline), cyclized from N-terminal glutamine. X marks a noncanonical residue; see the expanded sequence and reference chemistry below.

Analyze sequences in the playground →

Structure & chemistry

Molecular identity & reference confidence

Source-supported reference

Bombesin is the frog peptide; select the explicitly reviewed Bombina bombina 14-residue structure rather than a human gastrin-releasing peptide homolog. Both legacy CIDs independently have the same InChIKey and defined stereochemistry. The PubChem graph confirms both blocked termini.

Molecular form
Bombina bombina bombesin(1-14), N-terminal L-pyroglutamate and C-terminal Met amide
Species
Bombina bombina
Termini (N / C)
Blocked L-pyroglutamate lactam nitrogen / L-methionine carboxamide (-CONH2)

Average reference mass · Molecular identity assessment: 2026-10-05

Reference policy updated: 2026-10-05

Full sequence with modifications

L-pGlu-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2

Molecular formula
C71H110N24O18S
Average reference mass
≈ 1,619.9
Backbone
Bombina bombina bombesin(1-14), N-terminal L-pyroglutamate and C-terminal Met amide
C-terminus
L-methionine carboxamide (-CONH2)
Identifiers

Chemistry values: curated profile, PubChem.

Clinical development snapshot

ClinicalTrials.gov lists 31 registered studies with “Bombesin” as an intervention (snapshot 2026-10-01). A registry footprint is not evidence of efficacy or approval.

Registered studies
31
Highest phase reached
Phase 3
Active in latest 100
7
Most recent update
2026-09-22
Most recently updated studies
NCTTitlePhaseStatusUpdated
NCT06379217NEPC Study: An Exploratory Safety and Efficacy Study With PSMA, SSTR2 and GRPR Targeted Radioligand Therapy inPhase 1active not recruiting2026-09-22
NCT07828678PET/CT Imaging of GRPR Expression in Various TumorsEarly phase 1not yet recruiting2026-09-18
NCT05870579[177Lu]Lu-NeoB in Combination With Ribociclib and Fulvestrant in Participants With ER+, HER2- and GRPR+ AdvancPhase 1active not recruiting2026-09-11
NCT06247995A Phase I/II, Dose Finding and Optimization Study of [177Lu]Lu-NeoB in Combination With Capecitabine in PatienPhase 2active not recruiting2026-09-11
NCT05889728Pilot Trial to Assess 68Ga Bombesin PET/CT (NeoB) Imaging for Staging of Breast CancerPhase 2completed2026-08-19
NCT03872778[177Lu]-NeoB in Patients With Advanced Solid Tumors and With [68Ga]-neoB Lesion UptakePhase 2completed2026-07-28
See all on ClinicalTrials.gov →
Concentration math

Bombesin — reconstitution calculator

Enter how much peptide is in the vial and how much diluent (e.g. bacteriostatic water) is added. The tool returns the resulting solution concentration — and, for any amount you type, the volume it corresponds to. This is educational arithmetic, not a dosing recommendation.

Reference form: Bombina bombina bombesin(1-14), N-terminal L-pyroglutamate and C-terminal Met amideAverage reference mass: 1,619.9 Da

Syringe graduation
Solution concentration
5 mg/mL5,000 mcg/mL
mcg

Enter an amount to see the volume it corresponds to.

Educational concentration mathematics only. This tool does not recommend a dose, amount, or protocol, and nothing here is medical advice. Many peptides are not authorized by Health Canada for human use — see our reconstitution and bacteriostatic-water guides for context.

Open the Bombesin calculator on its own page →

Change log

Dated observations from the data pipeline (registry flags, trial footprints, identifiers) and editorial reviews of this profile.

  1. Trials1 registered study added on ClinicalTrials.gov (now 31).

FAQ about Bombesin

What is Bombesin?+

Bombesin is a 14-amino-acid peptide first isolated from amphibian skin that gave its name to a family of mammalian receptors. It is widely used as a research tool in appetite and receptor-biology studies.

What Canadian product status is recorded for Bombesin?+

Canadian product status for Bombesin has not been verified in this profile. No verified record here does not mean no authorization exists. Status depends on the product, formulation and use; consult Health Canada's product records.

What is the length of the selected reference form for Bombesin?+

The selected reference form (Bombina bombina bombesin(1-14), N-terminal L-pyroglutamate and C-terminal Met amide) has 14 residues or residue-derived units in its backbone. Other forms in this family may have a different length.

Related peptides

References & further reading

  1. 1.Martinez et al. (2000). Bombesin and the brain-gut axis. Peptides
  2. 2.Yamada et al. (2002). Bombesin and its family of peptides: prospects for the treatment of obesity. Eur J Pharmacol
  3. 3.Cowan et al. (1985). Effects of bombesin on behavior. Life Sci
  4. 4.Tache et al. (1985). Central nervous system action of bombesin to inhibit gastric acid secretion. Life Sci
  5. 5.Liehr et al. (1990). Direct vs. indirect effects of bombesin on pancreatic growth. Digestion
  6. 6.Hirooka et al. (2021). The gastrin-releasing peptide/bombesin system revisited by a reverse-evolutionary study considering Xenopus. Sci Rep
  7. 7.Zhang et al. (2014). Bombesin facilitates GABAergic transmission and depresses epileptiform activity in the entorhinal cortex. Hippocampus
  8. 8.Ashour et al. (2006). Bombesin inhibits alveolarization and promotes pulmonary fibrosis in newborn mice. Am J Respir Crit Care Med
  9. 9.PubChem — compound summary for Bombesin (CID 16201612)
  10. 10.Wikipedia — Bombesin
Disclaimer: Educational content only. Not medical advice. Not instructions for human use. Research peptides and unapproved products may be restricted or illegal to market for human consumption in your jurisdiction. Consult qualified professionals and applicable law.
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